Serial Daily Diaphragm Ultrasounds in Ventilated Patients

March 9, 2015 updated by: Steve Reynolds

Serial Ultrasonographic Evaluation Of Diaphragm Thickness During Mechanical Ventilation In ICU Patients

When a person is put on a breathing machine the investigators think that the breathing muscles can get weaker. The investigators are not sure how quickly this happens but in some people this leads to problems when they try to breathe on their own without the breathing machine. The diaphragm is at the bottom of a person's chest separating their lungs from what is in their belly and it is a very strong muscle. In fact, it is main muscle that one uses for breathing.

An ultrasound machine is a painless way to see what is happening beneath the skin. It is safe and easy to do. Using an ultrasound the investigators are planning to measure how thick the diaphragm is and how much it changes while a person is on a breathing machine in the ICU.

Getting a better understanding of this condition could lead to improved treatments that might help support patients who require a ventilator for breathing.

The investigators hypothesis is that patients for whom the breathing machine is doing all of the work of breathing, will have their diaphragm thickness gradually decrease and changing to a breathing modem mode where they have to put in more effort the diaphragm thickness will start increasing again.

Study Overview

Detailed Description

The investigators propose to expand the investigators single-centre longitudinal pilot study into a complete study in which the investigators will use B-mode ultrasonography to evaluate daily changes in diaphragm thickness in all critically ill patients on mechanical ventilation (MV) until successful weaned from MV. The impact of patient age, co-morbidities, and the use of various modes of ventilation on diaphragm thickness will be assessed. Diaphragmatic thickness and its change from baseline will be evaluated as predictors of the need for a prolonged wean (>7days).

The investigators hypothesize that in patients on mandatory mode ventilation, diaphragmatic thickness will progressively decrease. Switching from mandatory to assisted breathing modes will correlate with increases in diaphragmatic thickness.

Study Type

Observational

Enrollment (Actual)

61

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • British Columbia
      • New Westminster, British Columbia, Canada, V3L 3W7
        • Royal Columbian Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

19 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Mechanically ventilated critical ill patients

Description

Inclusion Criteria:

  • All patients age ≥19 years in the ICU on ventilation

Exclusion Criteria:

  • History of diaphragmatic or neuromuscular disease
  • On a home ventilator
  • History of diaphragm surgery
  • Absence of adequate initial US images (3 consecutive days with at least 2 operators)
  • BMI greater than 40

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Ventilation- mandatory mode only
those patient ventilator days during which they had only received a mandatory mode of ventilation
Patient days during which only a mandatory ventilation mode was used and prior to this no voluntary mode was used.
Ventilation- voluntary mode only
Those patient days on a mechanical ventilator who have not received prior mandatory ventilation during this episode of mechanical ventilation.
Patient days on a voluntary mode with no preceding days with a majority of time spend on a mandatory mode
voluntary with preceding mandatory
Those patient ventilator days where the patient had at least one prior day of mandatory mechanical ventilation during this episode of respiratory support.
Patient days on a voluntary vent mode with at least one day prior during which the majority of the vent mode was mandatory.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
US measurement of diaphragm and quadriceps thickness
Time Frame: Participants will be ultrasounded daily until they are extubated or the 3 month study period has ended, the expected average duration of mechanical ventilation is 4.4 days at our institution
Diaphragm thickness will be measured once per day and continue until extubation, liberation from mechanical ventilation, transfer to another facility, death, or study completion.
Participants will be ultrasounded daily until they are extubated or the 3 month study period has ended, the expected average duration of mechanical ventilation is 4.4 days at our institution

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Quadriceps muscle thickness
Time Frame: Participants will be ultrasounded daily until they are extubated or the 3 month study period has ended, the expected average duration of mechanical ventilation is 4.4 days at our institution
The thickness of the quadriceps muscle on ultrasound will be measured daily until patient exit from study
Participants will be ultrasounded daily until they are extubated or the 3 month study period has ended, the expected average duration of mechanical ventilation is 4.4 days at our institution
PEEP (Postive end expiratory pressure) applied by the mechanical ventilator at the time of the ultraspound
Time Frame: Participants will be ultrasounded daily until they are extubated or the 3 month study period has ended, the expected average duration of mechanical ventilation is 4.4 days at our institution
The PEEP (as described above in the title) in cm H20 as applied by the mechanical ventilator, measured at the time of ultrasound
Participants will be ultrasounded daily until they are extubated or the 3 month study period has ended, the expected average duration of mechanical ventilation is 4.4 days at our institution
re-intubated within 48 hours
Time Frame: followed for 48 hours post extubation, or 3 month study period has ended
Whether a patient required re-intubation within 48 hours of extubation
followed for 48 hours post extubation, or 3 month study period has ended
mean daily fluid balance
Time Frame: Will be recorded daily until they are extubated or the 3 month study period has ended, the expected average duration of mechanical ventilation is 4.4 days at our institution
Fluid balance of administer fluids minus measurable excreted fluid as recorded every 24 hours by the bedside nurse
Will be recorded daily until they are extubated or the 3 month study period has ended, the expected average duration of mechanical ventilation is 4.4 days at our institution
mean daily FiO2 (oxygen level administered)
Time Frame: Will be recorded daily until they are extubated or the 3 month study period has ended, the expected average duration of mechanical ventilation is 4.4 days at our institution
The daily average oxygen delivered through the mechanical ventilator to the patient.
Will be recorded daily until they are extubated or the 3 month study period has ended, the expected average duration of mechanical ventilation is 4.4 days at our institution
mode of mechanical ventilation for >80% of the day
Time Frame: Will be recorded daily until they are extubated or the 3 month study period has ended, the expected average duration of mechanical ventilation is 4.4 days at our institution
Mode of mechanical ventilation for the >80% of the day will be recorded here. This will be split into a mandatory mode (where the machine supplies a breath) or a voluntary mode (where the patient triggers the breath and the machine supports it).
Will be recorded daily until they are extubated or the 3 month study period has ended, the expected average duration of mechanical ventilation is 4.4 days at our institution
steroids given
Time Frame: Will be recorded daily until they are extubated or the 3 month study period has ended, the expected average duration of mechanical ventilation is 4.4 days at our institution
This will include any dose of steroids administered to the patient each day during their intubation.
Will be recorded daily until they are extubated or the 3 month study period has ended, the expected average duration of mechanical ventilation is 4.4 days at our institution
vasopressors given
Time Frame: Will be recorded daily until they are extubated or the 3 month study period has ended, the expected average duration of mechanical ventilation is 4.4 days at our institution
This will include any dose of medications to support the blood pressure (norepinephrine, epinephrine, dopamine, dobutamine, amrinone) administered to the patient each day during their intubation.
Will be recorded daily until they are extubated or the 3 month study period has ended, the expected average duration of mechanical ventilation is 4.4 days at our institution
paralytics given
Time Frame: Will be recorded daily until they are extubated or the 3 month study period has ended, the expected average duration of mechanical ventilation is 4.4 days at our institution
This will include any dose of paralytic medication administered to the patient each day during their intubation, except given as part of their initial intubation
Will be recorded daily until they are extubated or the 3 month study period has ended, the expected average duration of mechanical ventilation is 4.4 days at our institution
30 day mortality
Time Frame: 30 days after patient is extubated, or at the end of the follow up period 1 month after the 3 month study has ended
This is to capture all cause mortality. A patient will be considered to have survived if they are discharged from hospital.
30 days after patient is extubated, or at the end of the follow up period 1 month after the 3 month study has ended
Body Mass Index (BMI)
Time Frame: from admission information, at the time of admission to the ICU, obtained from the patient record
The standard BMI will be recorded as determined by the clinical dietician.
from admission information, at the time of admission to the ICU, obtained from the patient record
presence of sepsis/severe sepsis on admission
Time Frame: from admission information, at the time of admission to the ICU, obtained from the patient record.
This will be determined as positive if there is any reference to infection in the patients admitting paperwork in conjunction with the classic SIRS (systemic inflammatory response syndrome) criteria.
from admission information, at the time of admission to the ICU, obtained from the patient record.
% Caloric goals met in preceding 24 hours
Time Frame: Will be recorded daily until they are extubated or the 3 month study period has ended, the expected average duration of mechanical ventilation is 4.4 days at our institution
A % of caloric goals delivered over the preceding 24 hours will be captured
Will be recorded daily until they are extubated or the 3 month study period has ended, the expected average duration of mechanical ventilation is 4.4 days at our institution
Initial presence of malnutrition
Time Frame: Measure at the time of admission to the ICU
Presence of malnutrition as assessed by dietician on admission
Measure at the time of admission to the ICU
At risk for re-feeding syndrome
Time Frame: Assessed on admission to the ICU
Presence of risk for re-feeding syndrome as assessed by dietician on admission
Assessed on admission to the ICU

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Collaborators

Investigators

  • Principal Investigator: Steven Reynolds, MD, Royal Columbian Hospital, Fraser Health

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

June 1, 2014

Primary Completion (ACTUAL)

August 1, 2014

Study Completion (ACTUAL)

September 1, 2014

Study Registration Dates

First Submitted

May 27, 2014

First Submitted That Met QC Criteria

June 24, 2014

First Posted (ESTIMATE)

June 25, 2014

Study Record Updates

Last Update Posted (ESTIMATE)

March 11, 2015

Last Update Submitted That Met QC Criteria

March 9, 2015

Last Verified

March 1, 2015

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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